Results
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68101.
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68102.
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68103.
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Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus. [electronic resource] by
- Cacciagli, Pierre
- Sutera-Sardo, Julie
- Borges-Correia, Ana
- Roux, Jean-Christophe
- Dorboz, Imen
- Desvignes, Jean-Pierre
- Badens, Catherine
- Delepine, Marc
- Lathrop, Mark
- Cau, Pierre
- Lévy, Nicolas
- Girard, Nadine
- Sarda, Pierre
- Boespflug-Tanguy, Odile
- Villard, Laurent
Producer: 20131105
In:
American journal of human genetics vol. 93
Availability: No items available.
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68104.
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68105.
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68106.
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68107.
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68108.
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68109.
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68110.
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68111.
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68112.
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68113.
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68114.
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68115.
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68116.
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68117.
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68118.
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68120.
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